Aside

Bernt Popp

Kontakt

Competence

Disclaimer

Last change 2023-10-25.

Main

Dr. med. Bernt Popp

Curriculum Vitae

As a physician and scientist I am currently working at the University Hospital Leipzig and at the BIH at the Charité Berlin.

From a human genetics perspective, my scientific interests are in rare diseases of neuronal development, rare tumors and the kidney. I particularly enjoy working bioinformatically on the analysis of data from high-throughput sequencing and on the curation of genetic diseases, variants and genes.

Academic and medical-clinical career

Project lead Innovation in Human Genetics (Senior physician equivalent) at Labor Berlin — Charité Vivantes GmbH (50%)

Labor Berlin — Charité Vivantes GmbH

Berlin, Germany

since 01/2023

Department of Human Genetics at Labor Berlin — Charité Vivantes GmbH

Senior physician and Postdoc at Charité – Universitätsmedizin Berlin (50%)

Berlin Institute of Health (BIH)

Berlin, Germany

since 07/2022

Translational Research Area - Research Group “Hypertension and Molecular Biology of Endocrine Tumors” (Prof. Dr. med. Ute Scholl)

Senior physician and head of the genetics outpatient clinic at MVZ Dresden

Medizinisches Versorgungszentrum des Universitätsklinikums Dresden

Dresden, Germany

07/2021 - 04/2022

Head of the genetic outpatient clinic as senior physician

Specialist in Human Genetics

at the Institute of Human Genetics, University of Leipzig Medical Center, Leipzig, Germany

Leipzig, Germany

06/2021 - 04/2021

Deputy Team Leader Genetic Diagnostics - Clinical Genomics

Recognition as a specialist in Human Genetics

Completed specialist training and examination by the Saxony State Medical Association

Dresden, Germany

03/2021

Allowed to use the title “Specialist in Human Genetics” (German: “Facharzt für Humangenetik”)

DFG (German Research Foundation) rotation position

Scientific-medical assistant at the Human Genetics Institute of the University Hospital Leipzig

Leipzig, Germany

since 01/2020

Within the funds raised for the project “Exome Pool-Seq and systems biology approach to identify and characterize genes and networks in neurodevelopmental disorders”

Resident

at the Institute of Human Genetics, University of Leipzig Medical Center, Leipzig, Germany

Leipzig, Germany

03/2021 - 06/2019

Training as a specialist in human genetics

Clinical year

as an assistant physician in the field of nephrology at the Clinic and Polyclinic for Endocrinology, Nephrology, Rheumatology at the University Hospital Leipzig

Leipzig, Germany

09/2020 - 09/2019

Training as a specialist in human genetics

Resident and scientific-medical assistant

at the Institute of Human Genetics, University Hospital Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), Erlangen, Germany

Erlangen, Germany

05/2019 - 02/2013

Training as a specialist in human genetics

Dissertation Dr. med.

Institute of Human Genetics, University Hospital Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), Erlangen, Germany

Erlangen, Germany

05/2019 - 02/2013

Title of the dissertation „De novo missense mutations in the NAA10 gene cause severe non-syndromic developmental delay in males and females” (summa cum laude)

License as physician (Appropation)

after completing medical studies at the FAU Erlangen-Nuremberg

Erlangen, Germany

11/2012

Education

Part-time study Bachelor of Science Computer Science

at the state distance-learning university FernUniversität in Hagen

Hagen, Germany

10/2021 - 10/2019

Medical School

FAU Erlangen-Nürnberg (Staatsexamen)

Erlangen, Germany

11/2012 - 10/2005

General university entrance qualification (Allgemeine Hochschulreife)

Peter-Vischer-Gymnasium, Nuremberg

Nuremberg, Germany

06/2005 - 09/1996

Publications

A complete and always up-to-date list can be found at Google Scholar.